absent estrous cycle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure of female animals to enter or progress through the estrous cycle (Mammalian Phenotype Ontology, MP_0009009)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009009
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Genes

25 gene mutations causing the absent estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
ESR1 estrogen receptor 1
FANCL Fanconi anemia, complementation group L
FOXO3 forkhead box O3
FSHR follicle stimulating hormone receptor
GNRHR gonadotropin-releasing hormone receptor
IRS2 insulin receptor substrate 2
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LATS1 large tumor suppressor kinase 1
LEPR leptin receptor
LHB luteinizing hormone beta polypeptide
LHCGR luteinizing hormone/choriogonadotropin receptor
LHX9 LIM homeobox 9
NPC1 Niemann-Pick disease, type C1
NPR2 natriuretic peptide receptor 2
PER1 period circadian clock 1
PER2 period circadian clock 2
POSTN periostin, osteoblast specific factor
SIRT1 sirtuin 1
TSHR thyroid stimulating hormone receptor
VGF VGF nerve growth factor inducible